The role of a Lab Coordinator assists all team members of the clinical research team. The Lab Coordinator is responsible for ensuring all lab activities are completed timely, accurately, and per study protocol. This position includes but not limited to processing lab samples, shipping lab samples per protocol specification and timeline.
To consistently embody AMR Clinicals Core Values :
- United We Achieve
- Celebrate Diverse Perspectives
- Do the Right Thing
- Adapt and Persevere
The Lab Coordinator reports to the Site Manager / Lab Manager.
Classification : Non-Exempt
Primary Responsibilities :
Ensure Compliance with Regulatory & Safety Standards Adhere to Good Clinical Laboratory Practices (GCLP), ICH-GCP, FDA, IATA, and OSHA regulations when handling and processing specimens.Perform Quality Control Checks Regularly inspect sample processing, storage conditions, and lab documentation to ensure compliance and prevent deviations.Troubleshoot Lab Processing Issues Identify and resolve sample processing delays, equipment malfunctions, and protocol deviations to prevent disruptions.Support Sponsor & Monitor Requests Assist with remote and on-site lab monitoring visits, including document retrieval, sample reconciliation, and audit preparation.Develop & Implement Lab Training Programs Train new team members on lab protocols, safety measures, and compliance requirements.Collaborate with Study Teams to Optimize Workflows Work with monitors, clinical staff, CRCs, and regulatory teams to improve lab processes and efficiency.Draw labs and collect specimen per the study protocolProcess and store lab specimens per study protocolPackage lab specimens according to study protocol.Ship lab specimens per study protocolAnswer queries in a timely mannerInventory lab suppliesUnpack and put away supplies and study materials received from study sponsors.Maintain logs for refrigerator and freezersMaintain logs for required equipmentEnsure calibration is maintained on all equipmentComplete forms and study documents with accuracyClean and sanitize lab area dailyRemove subject identifying documents when assisting with remote monitoring activities.Assist clinical team with all study activities as needed. Such as vitals, EKGs, phlebotomy, etc.Maintain a safe work environment, meeting IATA and OSHA standards.Serve as a resource in lab for all team members to ensure protocols are followed.Position may require occasional weekend and / or overtime hours.Other duties as assignedDesired Skills and Qualifications :
Phlebotomy experience requiredLab processing experience requiredCollege graduate preferredAbility to troubleshoot lab equipment malfunctions and implement corrective actions.Familiarity with hazardous material handling and biosafety protocols.Excellent attention to detail, organizational skills, and ability to manage multiple priorities.Ability to function independently with little oversightProfessional, highly motivated self-starter, and exercises initiative.Collaborative with a team mentalityAbility to work fast-paced environmentOrganization and prioritization skillsExcellent follow-upAbility to be ambulatory most of the workday.Ability to lift / transfer / push / manipulate equipment and patients, which requires strength, gross motor and fine motor coordination.AMR Clinical does not discriminate in employment on the basis of race, color, religion, sex (including pregnancy and gender identity), national origin, political affiliation, sexual orientation, marital status, disability, genetic information, age, retaliation, parental status, military service, or other non-merit factor.
This job description is intended to be a representative summary of the major responsibilities and accountabilities of the staff holding this position. The staff may be requested to perform job-related tasks other than those stated in this description.Compensation details : 20-23 Hourly Wage
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